The present invention provides a bone cement composition comprising a bone matrix and a bone cement matrix formed by an acrylic polymer and an acrylic monomer, wherein the ratio of the bone matrix to the bone cement matrix is in a range from about 1:2 (g/g) to about 1:1000 (g/g). The present invention further provides a bone cement composition kit comprising a bone matrix component, a powder component, and a liquid component, respectively stored in separate containers, wherein the bone matrix component includes a bone matrix, the powder component includes an acrylic polymer, and the liquid component includes an acrylic monomer. The powder component and the liquid component are mixable to produce a bone cement matrix component. A ratio of the bone matrix component to the bone cement matrix component is in a range from about 1:2 (mL/mL) to about 1:50 (mL/mL).

The present invention provides a bone cement composition comprising a bone matrix and a bone cement matrix formed by an acrylic polymer and an acrylic monomer, wherein the ratio of the bone matrix to the bone cement matrix is in a range from about 1:2 (g/g) to about 1:1000 (g/g). The present invention further provides a bone cement composition kit comprising a bone matrix component, a powder component, and a liquid component, respectively stored in separate containers, wherein the bone matrix component includes a bone matrix, the powder component includes an acrylic polymer, and the liquid component includes an acrylic monomer. The powder component and the liquid component are mixable to produce a bone cement matrix component. A ratio of the bone matrix component to the bone cement matrix component is in a range from about 1:2 (mL/mL) to about 1:50 (mL/mL).

A cured hybrid magnesium cement (HMC) composition and an exemplary process for forming a cured HMC composition are disclosed. The cured HMC composition includes a magnesium-containing material, a metal silicate inorganic polymer having a repeat unit of SiP.sub.2O.sub.7, and a salt having a non-metallic oxide anion. The process includes first combining a mixture of magnesium-containing material, a metal silicate inorganic polymer having a repeat unit of SiP.sub.2O.sub.7, and a salt having a non-metallic oxide anion, and then mixing the mixture with water.

A mineral wool insulating product which comprises a layer, notably a continuous layer, of mixed mineral wool fibres, the mixed mineral wool fibres comprising a binder, first mineral wool fibres and second mineral wool fibres, the first mineral wool fibres and the second mineral wool fibres have a difference of softening point.

A calcium phosphate apatite cement-forming composition comprises an apatite-forming calcium-based precursor powder and from 1 to 30 wt %, based on the weight of the precursor powder, of dicalcium pyrophosphate powder or or sodium pyrophosphate powder. Apatite cements formed form such compositions may be used in implants for correcting bone defects. Methods for bone defect repair employ implants formed from such apatite cements and slow implant resorption and/or improve in vivo bone induction in a patient.

Provided is a fluoroaluminosilicate glass powder that can provide a dental glass ionomer cement hardened body excellent in acid resistance, the glass powder including sodium and potassium which have an effect of lowering the reflective index of glass. A mass ratio of potassium to sodium in the component is in the range of from 1.2 to 1.9 in terms of oxide.

The present invention disclosed a cross-linked plugging agent stimulated by high density brine which comprises: main agent: 21 wt %-53 wt %, gelling agent: 0.5 wt %-9 wt % and pure water; wherein the saline solution is selected from the group consisting of a Dipotassium phosphate (K.sub.2HPO.sub.4), a Tripotassium phosphate (K.sub.3PO.sub.4) and a Potassium pyrophosphate (K.sub.4P.sub.2O.sub.7); the gelling agent is selected from the group consisting of a Xanthan gum and a kappa carrageenan. The gelling time is controlled within 0.5-12 h under an experiment temperature of 90 C.-160 C. The final gelling strength is controlled within D-H. The density is controlled within 1.2-1.55 g/cm.sup.3.

The present invention disclosed a cross-linked plugging agent stimulated by high density brine which comprises: main agent: 21 wt %-53 wt %, gelling agent: 0.5 wt %-9 wt % and pure water; wherein the saline solution is selected from the group consisting of a Dipotassium phosphate (K.sub.2HPO.sub.4), a Tripotassium phosphate (K.sub.3PO.sub.4) and a Potassium pyrophosphate (K.sub.4P.sub.2O.sub.7); the gelling agent is selected from the group consisting of a Xanthan gum and a kappa carrageenan. The gelling time is controlled within 0.5-12 h under an experiment temperature of 90 C.-160 C. The final gelling strength is controlled within D-H. The density is controlled within 1.2-1.55 g/cm.sup.3.

Disclosed is a method of fabricating a construction element. The method may include assembling a mold on a rotational casting machine; rotating the mold around at least two axes at a predetermined speed; providing a first portion of magnesium silico-phosphate cement (MSPC) mix, having an altered hardening rate, to the mold while rotating the mold until at least a portion of the mold's walls is covered by a first layer of the MSPC mix; and rotating the mold until the MSPC mix is hardened to a predetermined degree.

The present disclosure is directed to a bioresorbable ceramic composition having a plurality of biocompatible ceramic granules, each of the granules having a coating of a plurality of calcium containing particles, where at least a portion of the particles are bound to at least a portion of an outer surface of each of the granules, and further where the composition is flowable in a dry state. The present disclosure is also directed to a three dimensional scaffold for bone repair that includes the bioresorbable composition, which upon implantation to a locus of repair defines an interconnected pore network between outer walls of the coated granules of the composition. Finally, the present disclosure is directed to methods of forming both the bioresorbable ceramic composition and the three-dimensional ceramic scaffold.